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NDC 72251-0002-74 Neova DNA Damage Control - Everyday 6.5; 2.5; 8.5 g/100mL; g/100mL; g/100mL Details
Neova DNA Damage Control - Everyday 6.5; 2.5; 8.5 g/100mL; g/100mL; g/100mL
Neova DNA Damage Control - Everyday is a TOPICAL EMULSION in the HUMAN OTC DRUG category. It is labeled and distributed by PHARMA COSMETICS, INC. The primary component is OCTINOXATE; OCTISALATE; ZINC OXIDE.
Product Information
| NDC | 72251-0002 |
|---|---|
| Product ID | 72251-002_075ea4f1-908c-3bd3-e063-6394a90a1cb7 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Neova DNA Damage Control - Everyday |
| Proprietary Name Suffix | Broad Spectrum SPF 44 |
| Non-Proprietary Name | Octinoxate, Octisalate, Zinc Oxide |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | EMULSION |
| Route | TOPICAL |
| Active Ingredient Strength | 6.5; 2.5; 8.5 |
| Active Ingredient Units | g/100mL; g/100mL; g/100mL |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Labeler Name | PHARMA COSMETICS, INC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M020 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72251-0002-74 (72251000274)
| NDC Package Code | 72251-002-74 |
|---|---|
| Billing NDC | 72251000274 |
| Package | 74 mL in 1 BOTTLE (72251-002-74) |
| Marketing Start Date | 2018-04-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |